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Traus Ssg30

FDA UDI

Class I (US FDA UDI)

by Saeshin Precision Co., Ltd.

Identity

Trade Name
TRAUS SSG30 FDA UDI
Generic Name
Dental laboratory power tool system FDA UDI
Model / Reference
SSG30 FDA UDI

Identifiers

Primary DI / UDI-DI
08809260473706 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Dental laboratory power tool system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental laboratory power tool system

Traus Ssg30 by Saeshin Precision Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental laboratory power tool system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7ee59b74-ff76-43b1-9fa3-f84e9d527d7e 32 fields · synced May 30, 2026